Label: AXE CREW CUT BUZZED LOOK WITH SUNSCREEN SPF 15- octinoxate, oxybenzone, octisalate cream

  • Category: HUMAN OTC DRUG LABEL

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated March 29, 2011

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  • ACTIVE INGREDIENT

    Active ingredients
    Octinoxate 7.0%, Oxybenzone 3.0%, Octisalate 1.0%
  • PURPOSE

    Purpose
    Sunscreen
  • INDICATIONS & USAGE

    Uses
    helps prevent sunburn
    higher SPF gives more sunburn protection
    provides moderate protection from sunburn
  • WARNINGS

    Warnings
    For external use only.
    If swallowed, get medical help or contact a Poison Control Center right away.

    When using this product keep out of eyes.  Rinse with water to remove.

    Stop use and ask a doctor if rash or irritation develops.

    Keep out of reach of children.
  • DOSAGE & ADMINISTRATION

    Directions
    Rub onto head and scalp before sun exposure and as needed.  Children under 6 months of age: ask a doctor.
  • INACTIVE INGREDIENT

    Inactive ingredients
    Water, Glycerin, Beeswax, Cetearyl Alcohol, Glyceryl Stearate, VP/VA Copolymer, Sodium Behenoyl Lactylate, Fragrance, Carbomer, Triethanolamine, DMDM Hydantoin, Disodium EDTA, Iodopropynyl Butylcarbamate.
  • QUESTIONS

    Questions?
    Visit us at www.TheAxeEffect.com or call us at 1-800-450-7580 Mon-Fri 8:30am - 6:00pm EST
  • PRINCIPAL DISPLAY PANEL

    Axe Buzzed Cut PDP front
    Axe Buzz SPF15 front PDP
  • PRINCIPAL DISPLAY PANEL

    Axe Buzz SPF15 back 1
    Axe Buzz SPF15 back 1
  • PRINCIPAL DISPLAY PANEL

    Axe Buzz SPF15 back 2
    Axe Buzz SPF15 back 2
  • PRINCIPAL DISPLAY PANEL

    Axe Buzz SPF15 back 3
    Axe Buzz SPF15 back 3
  • INGREDIENTS AND APPEARANCE
    AXE CREW CUT  BUZZED LOOK WITH SUNSCREEN SPF 15
    octinoxate, oxybenzone, octisalate cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:64942-1161
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE7.0 g  in 100 g
    OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) OXYBENZONE3.0 g  in 100 g
    OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE1.0 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    WHITE WAX (UNII: 7G1J5DA97F)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    DMDM HYDANTOIN (UNII: BYR0546TOW)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)  
    CARBOMER HOMOPOLYMER TYPE C (UNII: 4Q93RCW27E)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:64942-1161-175 g in 1 CONTAINER
    2NDC:64942-1161-215 g in 1 CONTAINER
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart35212/08/2010
    Labeler - CONOPCO Inc. d/b/a Unilever (001375088)
    Establishment
    NameAddressID/FEIBusiness Operations
    Conopco Inc. d/b/a Unilever198786444manufacture
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